| NDC Code | 68382-096-30 |
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| Package Description | 10 BLISTER PACK in 1 CARTON (68382-096-30) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
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| Product NDC | 68382-096 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Hydroxychloroquine Sulfate |
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| Non-Proprietary Name | Hydroxychloroquine Sulfate |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20080103 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040657 |
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| Manufacturer | Zydus Pharmaceuticals (USA) Inc. |
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| Substance Name | HYDROXYCHLOROQUINE SULFATE |
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| Strength | 200 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Antirheumatic Agent [EPC] |
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